Mission Regulatory Affairs Member

Excelya · posted Nov 4, 2026

Open to candidates in Bulgaria

Contract · Mid-level

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What this job asks for

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Must have

  • •3+ years of experience in Regulatory Affairs
  • •Familiarity with Bulgarian regulatory requirements
  • •Experience in EU regulatory submissions
  • •Fluent in English and Bulgarian
  • •Degree in Life Sciences

Nice to have

  • •Experience with pharmaceutical companies or consultancies

Languages required

bg

Read the full posting

Redefine Regulatory Affairs. Empower Innovation. Build with Audacity.

Join Excelya as Our Next RA Star!

At Excelya , we don’t just work—we Excelyate . Across 24 countries, 900+ passionate professionals are shaping the future of healthcare with one bold ambition: to become Europe's leading mid-size CRO, offering the best employee experience .

Now, we’re calling on curious minds and courageous spirits to step into a career-defining role in Regulatory Affairs . Ready to make an impact that travels the globe? Let’s talk.

About the Job

We are seeking a Freelancer Mission Regulatory Affairs Member, based in Bulgaria for a part-time, full remote role, to provide scientific expertise required for the successful completion of Excelya’s projects.

Your Mission:

  • To identify and communicate new Bulgarian legislation, amendments, guidelines and upcoming regulatory developments.
  • To provide expert input on Bulgarian regulatory requirements.
  • To manage EU regulatory submissions (DCP / MRP / National procedures).
  • To be responsible for the review and approval of:

o Mock-ups (artwork review)

o Translation of Product information texts

o Promotional materials in compliance with local regulations

What You Bring to the Table:

We are looking for candidates who embody our values of Audacity, Care, and Energy and also:

  • Degree in Life Sciences.
  • At least 3 years of experience in Regulatory Affairs.
  • Strong familiarity with local Regulatory requirements(as per Bulgarian Medicines Authority etc.) for pharmaceutical products for human use and medical devices.
  • Experience in EU regulatory submissions (DCP / MRP / National procedures).
  • Good understanding of EU regulatory framework and local regulations in Bulgaria.
  • Detail-oriented with strong compliance mindset.
  • Experience working with pharmaceutical companies or regulatory consultancies.
  • Able to work independently and deliver high-quality results within tight timelines.
  • Fluent in English and Bulgarian language.

Why Choose Excelya?

At Excelya, we lead with Audacity , act with Care , and move with Energy . We nurture your potential through high-impact projects, give your talents the space to shine, and push boundaries to elevate every patient’s journey. Here, you're not just doing a job—you’re becoming a key part of something bigger .

So, if you're ready to excel with purpose , let’s write the next chapter together.

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